Results 21 to 30 of about 500,057 (343)

Heavy-Chain Deposition Disease [PDF]

New England Journal of Medicine, 1993
Comment inOminous consequences of immunoglobulin deposition. [N Engl J Med. 1993]
Pièrre Aucouturier, Ahmed Amine Khamlichi, Guy Touchard, Eve Justrabo, Michel Cogné, Bruno Chauffert, F Martín, J L Preud'homme   +7 more
openalex   +4 more sources

Gamma heavy-chain disease accompanied with follicular lymphoma: a case report. [PDF]

Biochem Med (Zagreb), 2018
San-José P, Aguadero V, Perea G, Estrada M, Berlanga E.   +4 more
europepmc   +3 more sources

T cell receptor rearrangements in a patient with γ-heavy chain disease: A case report. [PDF]

Oncol Lett, 2016
Zhou H, Chen W, Zhang J, Zeng H, Jian Y, Fu C.   +5 more
europepmc   +3 more sources

Gamma-heavy chain disease [PDF]

Klinicka Onkologie, 2020
Gamma-heavy chain disease is a rare disease, described so far in approximately 150 cases. The aim of this work was laboratory dia-gnostics of immunoglobulin heavy chain disease.A 60-year-old patient was referred to the University Hospital in Ostrava for suspected marginal zone lymphoma from gastric bio-psy.
Tomas Jelinek, Roman Hájek, David Zeman, Pavlína Kušnierová   +3 more
openalex   +3 more sources

Alpha heavy chain disease [PDF]

Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2018
lpha heavy chain disease (HCD) is the most prevalent form of heavy chain diseases, a rare family of syndromes associated with or representing a B cell malignancy variant. The hallmark characteristic and the pathogenic mechanism of HCD is the synthesis of a mutant, misfolded immunoglobulin heavy chain (IgH) which cannot form a quaternary conformation ...
Giada Bianchi, Kenneth C. Anderson
openalex   +3 more sources

Gamma heavy chain disease lacks the MYD88 L265p mutation associated with lymphoplasmacytic lymphoma [PDF]

Haematologica, 2014
Fatima Hamadeh, Stephen MacNamara, Chris M Bacon, Aliyah R. Sohani, Steven H. Swerdlow, James R. Cook   +5 more
doaj   +2 more sources

Monoclonal gammopathy of renal significance: Spectrum of diseases and approach to a case

Saudi Journal of Kidney Diseases and Transplantation, 2021
The occurrence of kidney diseases associated with a monoclonal gammopathy in the absence of symptomatic multiple myeloma is increasingly recognized. When the kidney is involved, the monoclonal etiology of these diseases results in clinical and laboratory
Rohit Tewari, Tathagat Chatterjee, Satish Mendonca, Manu Dogra, Suman Kumar Pramanik, Uday Yanamandra   +5 more
doaj   +1 more source

Mutant glycyl-tRNA synthetase (Gars) ameliorates SOD1G93A motor neuron degeneration phenotype but has little affect on Loa dynein heavy chain mutant mice [PDF]

, 2009
Background: In humans, mutations in the enzyme glycyl-tRNA synthetase (GARS) cause motor and sensory axon loss in the peripheral nervous system, and clinical phenotypes ranging from Charcot-Marie-Tooth neuropathy to a severe infantile form of spinal ...
Antoni L. Andreu, Elizabeth M. C. Fisher, Francesca Achilli, Gareth T. Banks, Hazel P. Williams, J. Barney Bryson, Linda Greensmith, Ruth Chia, Virginie Bros-Facer   +8 more
core   +17 more sources

Heavy Chain Deposition Disease in Monoclonal Gammopathy of Renal Significance: A Prodrome of Multiple Myeloma Case and Literature Review. [PDF]

Cureus
Gnanasampanthan S, Samelis VP, Roufosse C, Kousios A.   +3 more
europepmc   +2 more sources

Franklin's disease: immunoglobulin heavy chain disease. [PDF]

Stem Cell Investig, 2015
A 64-year-old male presented with persistent fatigue, weakness and abdominal discomfort. He was found to have pancytopenia and hepatosplenomegaly. His bone marrow examination was mildly hypocellular with trilineage hematopoiesis. Serum protein electrophoresis revealed broad beta protein area but no gamma monoclonal spike (A).
Akinleye A, Nelson J, Islam H, Saeed F, Liu D.   +4 more
europepmc   +4 more sources